Monolayer films at high surface pressures are well-ordered, and due to
their 2D crystallinity they can act as sites of preferential nucleati
on. Recently it has been demonstrated that films at lower surface pres
sures can also be preferential nucleators, despite their decreased ord
ering. In this study we show that identifying the factors which can re
duce the interfacial tension is vital to understanding the varied mech
anisms through which nucleation beneath monolayer films can occur. In
particular, the preferential nucleation that is observed at low to med
ium surface pressures is explained by the compressible film rearrangin
g so as to minimize the lattice mismatch with the nucleating crystal f
ace, thereby reducing the interfacial tension of the system. We introd
uce a more quantitative approach in this paper to gain a greater insig
ht into this phenomenon. The nucleating species must be adsorbed upon
the film as a prerequisite for nucleation. We demonstrate that the ext
ent of this adsorption may be modeled using the appropriate Pi-A curve
s and an equation derived from the Gibbs and Langmuir adsorption isoth
erms. This approach also allows values for the adsorption energy and i
nterfacial tension for 100% adsorption to be estimated.